Hyperproinsulinemia

human disease

MedicalCondition rare_disease Q5958530

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Hyperproinsulinemia

Summary

Hyperproinsulinemia is a rare disease^[1].

Key Facts

Hyperproinsulinemia's instance of is recorded as rare disease^[2].
Hyperproinsulinemia's instance of is recorded as disease^[3].
Hyperproinsulinemia is a type of genetic disease^[4].
Hyperproinsulinemia is a type of diabetes^[5].
Hyperproinsulinemia's ICD-9-CM is recorded as 250.80^[6].
Hyperproinsulinemia's genetic association is recorded as INS^[7].

⭐ Popularity Graph

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Quick Facts

Instance of rare disease, class of disease

Subclass of genetic disease, diabetes

Properties

Genetic association INS

Icd-9-cm 250.80

External References (7)

Experimental factor ontology id 0009650

Mesh descriptor id C562776

Microsoft academic id (discontinued) 2779670698

Mondo id MONDO_0014535

Omim id 616214

Umls cui C0342283

Uniprot disease id DI-01585

🌐 Available in 2 languages

enHyperproinsulinemia ptHiperproinsulinemia

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

[2] ↑ Hyperproinsulinemia — instance of (P31): rare disease. wikidata.org.
[3] ↑ Hyperproinsulinemia — instance of (P31): disease. Familial hyperproinsulinemia. An autosomal dominant defect. wikidata.org.
[4] ↑ Hyperproinsulinemia — subclass of (P279): genetic disease. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[5] ↑ Hyperproinsulinemia — subclass of (P279): diabetes. wikidata.org.
[6] ↑ Hyperproinsulinemia — ICD-9-CM (P1692): 250.80. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[7] ↑ Hyperproinsulinemia — genetic association (P2293): INS. A structurally abnormal insulin causing human diabetes. Retrieved 2023-08-24. platform.opentargets.org. Provenance: wikidata.org.

Class ancestry

[1] ↑ Hyperproinsulinemia is an instance of rare disease (Q929833) [P31, primary]. Wikidata. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA

4ort.xyz Knowledge Graph. (2026). Hyperproinsulinemia. Retrieved May 3, 2026, from https://4ort.xyz/entity/hyperproinsulinemia

MLA “Hyperproinsulinemia.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/hyperproinsulinemia.

BibTeX

@misc{4ortxyz_hyperproinsulinemia_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Hyperproinsulinemia}}, year = {2026}, url = {https://4ort.xyz/entity/hyperproinsulinemia}, note = {Accessed: 2026-05-03}}

LLM prompt

According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Hyperproinsulinemia — https://4ort.xyz/entity/hyperproinsulinemia (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/hyperproinsulinemia · Last refreshed: May 3, 2026

Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

13d ago · JhealdBatch bot · 2026-07-04 view diff on Wikidata ↗

Mondo id → MONDO_0014535

Imported from → —

Umls cui → C0342283

Uniprot disease id → DI-01585

+ 9 other properties edited (see Wikidata diff for full list)

"/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39873|batch #39873]]: P31 = "type of disease""

Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.